US20110189818A1 - Method for forming oxide thin film transistor - Google Patents
Method for forming oxide thin film transistor Download PDFInfo
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- US20110189818A1 US20110189818A1 US12/774,562 US77456210A US2011189818A1 US 20110189818 A1 US20110189818 A1 US 20110189818A1 US 77456210 A US77456210 A US 77456210A US 2011189818 A1 US2011189818 A1 US 2011189818A1
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- 238000000034 method Methods 0.000 title claims abstract description 89
- 239000010409 thin film Substances 0.000 title claims abstract description 32
- 239000000758 substrate Substances 0.000 claims abstract description 44
- 239000004065 semiconductor Substances 0.000 claims abstract description 41
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 claims abstract description 40
- 238000000151 deposition Methods 0.000 claims abstract description 37
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910000077 silane Inorganic materials 0.000 claims abstract description 21
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 18
- 239000001272 nitrous oxide Substances 0.000 claims abstract description 18
- 229910052814 silicon oxide Inorganic materials 0.000 claims abstract description 18
- 239000010410 layer Substances 0.000 claims description 72
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 32
- 238000000623 plasma-assisted chemical vapour deposition Methods 0.000 claims description 23
- 239000011787 zinc oxide Substances 0.000 claims description 16
- 239000011241 protective layer Substances 0.000 claims description 12
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 claims description 11
- 229910052733 gallium Inorganic materials 0.000 claims description 11
- 229910052738 indium Inorganic materials 0.000 claims description 11
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 claims description 11
- JJTLZYRNWLKWIW-UHFFFAOYSA-N [Cu].[La].S=O Chemical compound [Cu].[La].S=O JJTLZYRNWLKWIW-UHFFFAOYSA-N 0.000 claims description 5
- PBAJOOJQFFMVGM-UHFFFAOYSA-N [Cu]=O.[Sr] Chemical compound [Cu]=O.[Sr] PBAJOOJQFFMVGM-UHFFFAOYSA-N 0.000 claims description 5
- UNRNJMFGIMDYKL-UHFFFAOYSA-N aluminum copper oxygen(2-) Chemical compound [O-2].[Al+3].[Cu+2] UNRNJMFGIMDYKL-UHFFFAOYSA-N 0.000 claims description 5
- HPSHZZDEEIEFFA-UHFFFAOYSA-N chromium;oxotin Chemical compound [Cr].[Sn]=O HPSHZZDEEIEFFA-UHFFFAOYSA-N 0.000 claims description 5
- YZZNJYQZJKSEER-UHFFFAOYSA-N gallium tin Chemical compound [Ga].[Sn] YZZNJYQZJKSEER-UHFFFAOYSA-N 0.000 claims description 5
- YULBFWISFJEMQB-UHFFFAOYSA-N oxotin titanium Chemical compound [Sn]=O.[Ti] YULBFWISFJEMQB-UHFFFAOYSA-N 0.000 claims description 5
- KYKLWYKWCAYAJY-UHFFFAOYSA-N oxotin;zinc Chemical compound [Zn].[Sn]=O KYKLWYKWCAYAJY-UHFFFAOYSA-N 0.000 claims description 5
- 229910001887 tin oxide Inorganic materials 0.000 claims description 5
- 239000011521 glass Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 15
- 239000001301 oxygen Substances 0.000 description 15
- 229910052760 oxygen Inorganic materials 0.000 description 15
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 11
- 239000007789 gas Substances 0.000 description 11
- 229910052710 silicon Inorganic materials 0.000 description 11
- 239000010703 silicon Substances 0.000 description 11
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 8
- 239000004020 conductor Substances 0.000 description 6
- 229910021417 amorphous silicon Inorganic materials 0.000 description 5
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 4
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 238000005229 chemical vapour deposition Methods 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000002736 metal compounds Chemical class 0.000 description 4
- 239000007800 oxidant agent Substances 0.000 description 4
- 230000001590 oxidative effect Effects 0.000 description 4
- 238000005240 physical vapour deposition Methods 0.000 description 4
- 150000003377 silicon compounds Chemical class 0.000 description 4
- MAKDTFFYCIMFQP-UHFFFAOYSA-N titanium tungsten Chemical compound [Ti].[W] MAKDTFFYCIMFQP-UHFFFAOYSA-N 0.000 description 4
- 238000010586 diagram Methods 0.000 description 3
- 229920001621 AMOLED Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 229910052786 argon Inorganic materials 0.000 description 2
- -1 for example Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- DOTMOQHOJINYBL-UHFFFAOYSA-N molecular nitrogen;molecular oxygen Chemical compound N#N.O=O DOTMOQHOJINYBL-UHFFFAOYSA-N 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 238000006479 redox reaction Methods 0.000 description 2
- QEERNBBWTNUCAW-UHFFFAOYSA-N [Si].N#[N+][O-] Chemical compound [Si].N#[N+][O-] QEERNBBWTNUCAW-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
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- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/7869—Thin film transistors, i.e. transistors with a channel being at least partly a thin film having a semiconductor body comprising an oxide semiconductor material, e.g. zinc oxide, copper aluminium oxide, cadmium stannate
- H01L29/78693—Thin film transistors, i.e. transistors with a channel being at least partly a thin film having a semiconductor body comprising an oxide semiconductor material, e.g. zinc oxide, copper aluminium oxide, cadmium stannate the semiconducting oxide being amorphous
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/7869—Thin film transistors, i.e. transistors with a channel being at least partly a thin film having a semiconductor body comprising an oxide semiconductor material, e.g. zinc oxide, copper aluminium oxide, cadmium stannate
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H01L21/02274—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/34—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies not provided for in groups H01L21/0405, H01L21/0445, H01L21/06, H01L21/16 and H01L21/18 with or without impurities, e.g. doping materials
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- H01L29/02—Semiconductor bodies ; Multistep manufacturing processes therefor
- H01L29/06—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions
- H01L29/10—Semiconductor bodies ; Multistep manufacturing processes therefor characterised by their shape; characterised by the shapes, relative sizes, or dispositions of the semiconductor regions ; characterised by the concentration or distribution of impurities within semiconductor regions with semiconductor regions connected to an electrode not carrying current to be rectified, amplified or switched and such electrode being part of a semiconductor device which comprises three or more electrodes
- H01L29/107—Substrate region of field-effect devices
- H01L29/1075—Substrate region of field-effect devices of field-effect transistors
- H01L29/1079—Substrate region of field-effect devices of field-effect transistors with insulated gate
- H01L29/1083—Substrate region of field-effect devices of field-effect transistors with insulated gate with an inactive supplementary region, e.g. for preventing punch-through, improving capacity effect or leakage current
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- H01L29/40—Electrodes ; Multistep manufacturing processes therefor
- H01L29/43—Electrodes ; Multistep manufacturing processes therefor characterised by the materials of which they are formed
- H01L29/49—Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET
- H01L29/4908—Metal-insulator-semiconductor electrodes, e.g. gates of MOSFET for thin film semiconductor, e.g. gate of TFT
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- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/66007—Multistep manufacturing processes
- H01L29/66969—Multistep manufacturing processes of devices having semiconductor bodies not comprising group 14 or group 13/15 materials
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- H—ELECTRICITY
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- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
- H01L29/66—Types of semiconductor device ; Multistep manufacturing processes therefor
- H01L29/68—Types of semiconductor device ; Multistep manufacturing processes therefor controllable by only the electric current supplied, or only the electric potential applied, to an electrode which does not carry the current to be rectified, amplified or switched
- H01L29/76—Unipolar devices, e.g. field effect transistors
- H01L29/772—Field effect transistors
- H01L29/78—Field effect transistors with field effect produced by an insulated gate
- H01L29/786—Thin film transistors, i.e. transistors with a channel being at least partly a thin film
- H01L29/78606—Thin film transistors, i.e. transistors with a channel being at least partly a thin film with supplementary region or layer in the thin film or in the insulated bulk substrate supporting it for controlling or increasing the safety of the device
- H01L29/78609—Thin film transistors, i.e. transistors with a channel being at least partly a thin film with supplementary region or layer in the thin film or in the insulated bulk substrate supporting it for controlling or increasing the safety of the device for preventing leakage current
Definitions
- the present invention relates to a method for forming thin film transistors, and in particular to a method for forming oxide thin film transistors.
- Thin film transistor display devices such as thin film transistor liquid crystal displays (TFT LCD), electrphoretic displays (EPD) and organic light emitting diode displays (OLED) are widely employed in various electronic applications, for example, small size applications such as mobile phones, and great size (e.g., 40 inches) television sets.
- TFT LCD thin film transistor liquid crystal displays
- EPD electrphoretic displays
- OLED organic light emitting diode displays
- a-Si amorphous silicon
- AMOLED active-matrix organic light-emitting diode
- Vg-Id voltage-current characteristic curve of a transistor applied in a conventional TFT LCD
- the leakage current is generally between 10 ⁇ 12 amperes (A) and 10 ⁇ 14 A, and is difficult to be less than 10 ⁇ 14 A.
- conventional a-Si is also not competent for such applications.
- the stability of a-Si is low and is not easy to meet the standards of mass production.
- LTPS Low temperature poly-silicon
- Oxide transistors have the advantages of high electron mobility and high stability, and can solve above problems. However, because the oxygen contained in the oxide semiconductor, a redox reaction easily occurs in the manufacturing process. Thus, there is a desire to provide a manufacturing process that can prevent the redox reaction of the oxide semiconductor and the obtained transistors have the advantages of low current leakage and high electron mobility.
- the present invention provides a method for forming oxide thin film transistors than can overcome aforementioned problems.
- An embodiment of the present invention provides a method for forming oxide thin film transistors, which includes the steps of: forming a gate electrode, a drain electrode, a source electrode, and an oxide semiconductor layer respectively.
- the oxide semiconductor layer is formed on the gate electrode; the drain electrode and the source electrode are formed at two opposite sides of the oxide semiconductor layer.
- the method further includes a step of depositing at least one dielectric layer of silicon oxide, and a reacting gas for depositing the silicon oxide includes silane and nitrous oxide.
- a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- Another embodiment of the present invention also provides a method for forming oxide thin film transistors, which includes the steps of: providing a substrate; forming a gate electrode on an upper surface of the substrate; performing a first depositing process to form a gate dielectric layer on a portion of the upper surface of the substrate and the gate electrode; forming an oxide semiconductor layer on the gate dielectric layer; forming a source electrode and a drain electrode on the oxide semiconductor layer; performing a second depositing process to form a protective layer covering the substrate, the source electrode, the drain electrode, and the oxide semiconductor layer.
- a reacting gas for at least one of the first and second depositing process includes silane and nitrous oxide, and a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- Another embodiment of the present invention also provides a method for forming oxide thin film transistors, which includes the steps of: providing a substrate; forming a source electrode and a drain electrode on the substrate; forming an oxide semiconductor layer on the substrate to connect the source electrode and the drain electrode; performing a first depositing process to form a gate dielectric layer to cover the substrate, the source electrode, the drain electrode and the oxide semiconductor layer; forming a gate electrode on the gate dielectric layer; performing a second depositing process to form a protective layer to cover the gate electrode and the gate dielectric layer.
- the gate dielectric layer and the protective layer are comprised of silicon oxide.
- a reacting gas for at least one of the first and second depositing process includes silane and nitrous oxide, and a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- a flow rate of the silane is in the range from 0.5 to 5 SCCM.
- the depositing process is plasma enhanced chemical vapor deposition (PECVD).
- PECVD plasma enhanced chemical vapor deposition
- an electric power applied in the depositing process is in the range from 0.5 KW to 10 KW.
- the oxide semiconductor layer comprises zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, or lanthanum copper oxysulfide.
- oxide thin film transistors manufactured by above method has advantages of low current leakage, high electron mobility, and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device.
- FIG. 1 is a scatter diagram showing the voltage-current (Vg-Id) characteristic curve of a transistor applied in a conventional TFT LCD.
- FIGS. 2 through 7 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with a first embodiment of the present invention.
- FIG. 8 is a scatter diagram showing the Vg-Id characteristic of the oxide thin film transistor manufactured by above method.
- FIGS. 9 through 14 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with the second embodiment of the present invention.
- FIGS. 2 through 7 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with a first embodiment of the present invention. The method will be described in detail accompanying with FIGS. 2 through 7 as follows.
- a substrate 10 is provided.
- the substrate 10 has an upper surface 101 for supporting other layers formed thereon.
- the substrate 10 can comprise different materials, for example, silicon, acrylic resin, or glass.
- the substrate 10 can be a transparent substrate such as a glass substrate.
- a gate electrode 11 is formed on the upper surface 101 of the substrate 10 .
- the gate electrode 11 can be formed by depositing a layer of electrically conductive material on the upper surface and then pattering the layer of electrically conductive material.
- the electrically conductive material can be doped silicon, aluminum, and copper; or metal compound such as titanium nitride or tungsten titanium.
- This step of forming the electrode 11 can include, but not limited to, forming scanning lines, capacitive bottom electrodes and/or common electrodes (not shown).
- the gate electrode 11 can be electrically connected to the scanning lines or is a part of the scanning lines.
- a first depositing process is performed to form a gate dielectric layer 12 on a portion of the upper surface 101 that is not covered by the gate electrode 11 and the gate electrode 11 .
- the gate dielectric layer 12 is preferably, but not limited to be, comprised of silicon oxide.
- the gate dielectric layer can include other oxide layer such as a silicon nitrous oxide layer.
- silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NO x ) as an oxygen source.
- the first depositing process includes physical vapor deposition or chemical vapor deposition.
- the first depositing process is plasma enhanced chemical vapor deposition (PECVD), and a reacting gas used in the PECVD process includes silane and nitrogen oxygen.
- a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM) such that the obtained gate dielectric layer 12 has better performance.
- SCCM standard cubic centimeters per minute
- a flow rate of nitrous oxide is in the range from 0.5 to 5 SCCM
- an electric power applied in the PECVD process is in the range from 0.5 kilowatt (KW) to 10 KW.
- the thickness of the obtained gate dielectric layer 12 is in the range from 300 angstroms ( ⁇ ) to 5000 ⁇ .
- an oxide semiconductor layer 13 is formed on the gate dielectric layer 12 .
- the oxide semiconductor layer 13 is the channel layer of the transistor, and the material of the oxide semiconductor 13 can comprise zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, and lanthanum copper oxysulfide.
- the oxide semiconductor layer 13 can be indium gallium zinc oxide, and a flow rate of argon gas used in the process for forming the indium gallium zinc oxide is 50 SCCM, an electric power is 3.5 KW, a volume ratio of oxygen in the reacting gas for forming the indium gallium zinc oxide is 9%.
- an ion implanting process can also be performed to dope ions into the channel area thereby controlling the conductivity of the transistor.
- the method can also include forming a doped source area and a doped drain area of the oxide semiconductor layer 13 .
- a source electrode 14 and a drain electrode 15 are formed on the oxide semiconductor layer 13 .
- the source electrode 14 and the drain electrode 15 can comprise doped silicon, copper or aluminum, or metal compounds such as titanium nitride, tungsten titanium.
- This step of forming the source electrode 14 and the drain electrode 15 can include, but is not limited to be, forming data lines and/or capacitive top electrode (not shown).
- the drain electrode 14 can be electrically connected to the data lines or is a part of the data lines.
- a second depositing process is performed to form a protective layer 16 to cover the substrate 10 , the source electrode 14 , the drain electrode 15 and the oxide semiconductor layer 13 .
- the protective layer 16 can comprise, but is not limited to, silicon oxide.
- the protective layer 16 can comprise other oxide such as silicon oxynitride.
- silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NO x ) as an oxygen source, and the depositing process for silicon oxide can be physical vapor deposition or chemical vapor deposition.
- the second depositing process is PECVD process
- the reacting gas includes silane and nitrous oxygen and the flow rate of nitrous oxygen is in the range 10 SCCM to 200 SCCM.
- the flow rate of silane is in the range from 0.5 SCCM to 5 SCCM.
- the electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW.
- the thickness of the obtained gate dielectric layer 12 is in the range from 300 ⁇ to 5000 ⁇ .
- a bottom gate oxide semiconductor transistor is obtained.
- FIG. 8 which shows a Vg-Id characteristic of the oxide thin film transistor manufactured by above method, the current leakage can be less than 10 ⁇ 14 A.
- the oxide thin film transistor also employs oxide semiconductor as the core thereof and thus has the advantages of high electron mobility and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device.
- FIGS. 9 through 14 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with the second embodiment of the present invention. The method will be described in detail accompanying with FIGS. 9 through 14 as follows.
- a substrate 20 is provided.
- the substrate 20 has an upper surface 201 for supporting other layers sequentially formed thereon.
- the substrate 20 can comprise different materials, for example, silicon, acrylic resin, or glass.
- the substrate 20 can be a transparent substrate such as a glass substrate.
- a source electrode 21 and a drain electrode 22 are formed on the substrate 20 .
- the source electrode 21 and the drain electrode 22 can comprise doped silicon, copper or aluminum, or metal compounds such as titanium nitride, tungsten titanium.
- an oxide semiconductor layer 23 is formed on the substrate 20 to connect the source electrode 21 and the drain electrode 22 .
- the oxide semiconductor layer 23 is the channel layer of the transistor to be formed, and can comprise zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, and lanthanum copper oxysulfide.
- the oxide semiconductor layer 23 can comprise indium gallium zinc oxide, and a flow rate of argon gas used in the process for forming the indium gallium zinc oxide is 50 SCCM, an electric power is 3.5 KW, a volume ratio of oxygen in the reacting gas for forming the indium gallium zinc oxide is 9%.
- a first depositing process is performed to form a gate dielectric layer 24 to cover the substrate 20 , the source electrode 21 , the drain electrode 22 , and the oxide semiconductor layer 23 .
- the gate dielectric layer 24 is preferably, but not limited to be, comprised of silicon oxide.
- silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NO x ) as an oxygen source.
- TEOS tetraethoxysilane
- silane silane
- an oxidant for example oxygen, ozone, oxynitride (NO x ) as an oxygen source.
- the first depositing process includes physical vapor deposition and chemical vapor deposition.
- the first depositing process is plasma enhanced chemical vapor deposition (PECVD), and a reacting gas used in the PECVD process includes silane and nitrogen oxygen.
- a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM) such that the obtained gate dielectric layer 12 has better performance.
- SCCM standard cubic centimeters per minute
- a flow rate of nitrous oxide is in the range from 0.5 to 5 SCCM
- an electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW.
- the thickness of the obtained gate dielectric layer 12 is in the range from 300 angstroms ( ⁇ ) to 5000 ⁇ .
- a gate electrode 25 corresponding to the oxide semiconductor layer 23 is formed on gate dielectric layer 24 .
- the gate electrode 25 can be formed by depositing a layer of electrically conductive material on gate dielectric layer 24 and then pattering the layer of electrically conductive material.
- the electrically conductive material can be doped silicon, aluminum, and copper; or metal compound such as titanium nitride or tungsten titanium.
- a second depositing process is performed to form a protective layer 26 to cover the gate electrode 25 and the gate dielectric layer 24 .
- the protective layer 26 can comprise, but is not limited to, silicon oxide.
- silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NO x ) as an oxygen source, and the depositing process for silicon oxide can be physical vapor deposition or chemical vapor deposition.
- the second depositing process is PECVD process
- the reacting gas includes silane and nitrous oxygen and the flow rate of nitrous oxygen is in the range 10 SCCM to 200 SCCM.
- the flow rate of silane is in the range from 0.5 SCCM to 5 SCCM.
- the electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW.
- the thickness of the obtained gate dielectric layer 24 is in the range from 300 ⁇ to 5000 ⁇ . According to above method, a top gate oxide thin film transistor is obtained.
- the top gate transistor is better than bottom gate transistor in this consideration.
- the bottom gate transistor is also acceptable. Both top gate transistors and bottom gate transistors can be applied in reflective display devices, in particular electro-phoretic display devices.
- the oxide thin film transistor manufactured using above method has advantages of low current leakage, high electron mobility, and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device.
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Abstract
Description
- This application claims the right of priority based on Taiwan Patent Application No. 099102730 entitled “Method for Forming Oxide Thin Film Transistor”, filed on Jan. 29, 2010, which is incorporated herein by reference and assigned to the assignee herein.
- 1. Technical Field
- The present invention relates to a method for forming thin film transistors, and in particular to a method for forming oxide thin film transistors.
- 2. Related Art
- Thin film transistor display devices such as thin film transistor liquid crystal displays (TFT LCD), electrphoretic displays (EPD) and organic light emitting diode displays (OLED) are widely employed in various electronic applications, for example, small size applications such as mobile phones, and great size (e.g., 40 inches) television sets. Thus, the studying and development of the structure and manufacturing process of thin film transistors are always of concern to people.
- Conventional technique of employing amorphous silicon (a-Si) as the core of the transistors can't meet the requirements in some fields. For example, the electron mobility of a-Si is generally less than 1 square centimeter per volt second (cm2/V•sec). However, in applications that require high electron mobility such as active-matrix organic light-emitting diode (AMOLED), the electron mobility should reach to or greater than 2 cm2/V•sec. For current leakage, referring to
FIG. 1 , which is a scatter diagram showing the voltage-current (Vg-Id) characteristic curve of a transistor applied in a conventional TFT LCD, it is illustrated that the leakage current is generally between 10−12 amperes (A) and 10−14 A, and is difficult to be less than 10−14 A. In addition, in order to simplify the manufacturing process and the structure, the technique of directly integrating other circuit member and functions on the thin film transistors substrate is developed out. However, conventional a-Si is also not competent for such applications. Besides, the stability of a-Si is low and is not easy to meet the standards of mass production. - Low temperature poly-silicon (LTPS) can overcome aforementioned problems, however the manufacturing process of LTPS is hard and the yield rate is low, and thus it is difficult to apply LTPS in commercial products.
- Oxide transistors have the advantages of high electron mobility and high stability, and can solve above problems. However, because the oxygen contained in the oxide semiconductor, a redox reaction easily occurs in the manufacturing process. Thus, there is a desire to provide a manufacturing process that can prevent the redox reaction of the oxide semiconductor and the obtained transistors have the advantages of low current leakage and high electron mobility.
- The present invention provides a method for forming oxide thin film transistors than can overcome aforementioned problems.
- An embodiment of the present invention provides a method for forming oxide thin film transistors, which includes the steps of: forming a gate electrode, a drain electrode, a source electrode, and an oxide semiconductor layer respectively. The oxide semiconductor layer is formed on the gate electrode; the drain electrode and the source electrode are formed at two opposite sides of the oxide semiconductor layer. The method further includes a step of depositing at least one dielectric layer of silicon oxide, and a reacting gas for depositing the silicon oxide includes silane and nitrous oxide. A flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- Another embodiment of the present invention also provides a method for forming oxide thin film transistors, which includes the steps of: providing a substrate; forming a gate electrode on an upper surface of the substrate; performing a first depositing process to form a gate dielectric layer on a portion of the upper surface of the substrate and the gate electrode; forming an oxide semiconductor layer on the gate dielectric layer; forming a source electrode and a drain electrode on the oxide semiconductor layer; performing a second depositing process to form a protective layer covering the substrate, the source electrode, the drain electrode, and the oxide semiconductor layer. A reacting gas for at least one of the first and second depositing process includes silane and nitrous oxide, and a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- Another embodiment of the present invention also provides a method for forming oxide thin film transistors, which includes the steps of: providing a substrate; forming a source electrode and a drain electrode on the substrate; forming an oxide semiconductor layer on the substrate to connect the source electrode and the drain electrode; performing a first depositing process to form a gate dielectric layer to cover the substrate, the source electrode, the drain electrode and the oxide semiconductor layer; forming a gate electrode on the gate dielectric layer; performing a second depositing process to form a protective layer to cover the gate electrode and the gate dielectric layer. The gate dielectric layer and the protective layer are comprised of silicon oxide. A reacting gas for at least one of the first and second depositing process includes silane and nitrous oxide, and a flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM).
- In another embodiment of the present invention, a flow rate of the silane is in the range from 0.5 to 5 SCCM.
- In another embodiment of the present invention, the depositing process is plasma enhanced chemical vapor deposition (PECVD).
- In another embodiment of the present invention, an electric power applied in the depositing process is in the range from 0.5 KW to 10 KW.
- In another embodiment of the present invention, the oxide semiconductor layer comprises zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, or lanthanum copper oxysulfide.
- According to measuring results, oxide thin film transistors manufactured by above method has advantages of low current leakage, high electron mobility, and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device.
- Other aspects, details, and advantages of the present method for forming transistors having oxide semiconductor layer are further described accompanying with preferred embodiments and figures as follows.
- These and other features and advantages of the various embodiments disclosed herein will be better understood with respect to the following description and drawings, in which like numbers refer to like parts throughout, and in which:
-
FIG. 1 is a scatter diagram showing the voltage-current (Vg-Id) characteristic curve of a transistor applied in a conventional TFT LCD. -
FIGS. 2 through 7 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with a first embodiment of the present invention. -
FIG. 8 is a scatter diagram showing the Vg-Id characteristic of the oxide thin film transistor manufactured by above method. -
FIGS. 9 through 14 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with the second embodiment of the present invention. - Referring to
FIGS. 2 through 7 ,FIGS. 2 through 7 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with a first embodiment of the present invention. The method will be described in detail accompanying withFIGS. 2 through 7 as follows. - Referring to
FIG. 2 , asubstrate 10 is provided. Thesubstrate 10 has anupper surface 101 for supporting other layers formed thereon. According to different applications, thesubstrate 10 can comprise different materials, for example, silicon, acrylic resin, or glass. For TFT LCD or EPD applications, thesubstrate 10 can be a transparent substrate such as a glass substrate. - Referring to
FIG. 3 , agate electrode 11 is formed on theupper surface 101 of thesubstrate 10. Thegate electrode 11 can be formed by depositing a layer of electrically conductive material on the upper surface and then pattering the layer of electrically conductive material. For example, the electrically conductive material can be doped silicon, aluminum, and copper; or metal compound such as titanium nitride or tungsten titanium. This step of forming theelectrode 11 can include, but not limited to, forming scanning lines, capacitive bottom electrodes and/or common electrodes (not shown). Thegate electrode 11 can be electrically connected to the scanning lines or is a part of the scanning lines. - Referring to
FIG. 4 , after that, a first depositing process is performed to form a gatedielectric layer 12 on a portion of theupper surface 101 that is not covered by thegate electrode 11 and thegate electrode 11. The gatedielectric layer 12 is preferably, but not limited to be, comprised of silicon oxide. In another embodiment, the gate dielectric layer can include other oxide layer such as a silicon nitrous oxide layer. Generally, silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NOx) as an oxygen source. The first depositing process includes physical vapor deposition or chemical vapor deposition. - In the present embodiment, the first depositing process is plasma enhanced chemical vapor deposition (PECVD), and a reacting gas used in the PECVD process includes silane and nitrogen oxygen. A flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM) such that the obtained gate
dielectric layer 12 has better performance. In other embodiment, a flow rate of nitrous oxide is in the range from 0.5 to 5 SCCM, an electric power applied in the PECVD process is in the range from 0.5 kilowatt (KW) to 10 KW. The thickness of the obtainedgate dielectric layer 12 is in the range from 300 angstroms (Å) to 5000 Å. - As shown in
FIG. 5 , then anoxide semiconductor layer 13 is formed on thegate dielectric layer 12. Theoxide semiconductor layer 13 is the channel layer of the transistor, and the material of theoxide semiconductor 13 can comprise zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, and lanthanum copper oxysulfide. In the present embodiment of the present invention, theoxide semiconductor layer 13 can be indium gallium zinc oxide, and a flow rate of argon gas used in the process for forming the indium gallium zinc oxide is 50 SCCM, an electric power is 3.5 KW, a volume ratio of oxygen in the reacting gas for forming the indium gallium zinc oxide is 9%. After theoxide semiconductor layer 13 is deposited, an ion implanting process can also be performed to dope ions into the channel area thereby controlling the conductivity of the transistor. In another embodiment, the method can also include forming a doped source area and a doped drain area of theoxide semiconductor layer 13. - Referring to
FIG. 6 , asource electrode 14 and adrain electrode 15 are formed on theoxide semiconductor layer 13. Thesource electrode 14 and thedrain electrode 15 can comprise doped silicon, copper or aluminum, or metal compounds such as titanium nitride, tungsten titanium. This step of forming thesource electrode 14 and thedrain electrode 15 can include, but is not limited to be, forming data lines and/or capacitive top electrode (not shown). Thedrain electrode 14 can be electrically connected to the data lines or is a part of the data lines. - Referring to
FIG. 7 , a second depositing process is performed to form aprotective layer 16 to cover thesubstrate 10, thesource electrode 14, thedrain electrode 15 and theoxide semiconductor layer 13. Theprotective layer 16 can comprise, but is not limited to, silicon oxide. In another embodiment, theprotective layer 16 can comprise other oxide such as silicon oxynitride. Generally, silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NOx) as an oxygen source, and the depositing process for silicon oxide can be physical vapor deposition or chemical vapor deposition. - In the present embodiment, the second depositing process is PECVD process, the reacting gas includes silane and nitrous oxygen and the flow rate of nitrous oxygen is in the
range 10 SCCM to 200 SCCM. The flow rate of silane is in the range from 0.5 SCCM to 5 SCCM. The electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW. The thickness of the obtainedgate dielectric layer 12 is in the range from 300 Å to 5000 Å. - According to above described method, a bottom gate oxide semiconductor transistor is obtained. As shown in
FIG. 8 , which shows a Vg-Id characteristic of the oxide thin film transistor manufactured by above method, the current leakage can be less than 10−14 A. Furthermore, the oxide thin film transistor also employs oxide semiconductor as the core thereof and thus has the advantages of high electron mobility and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device. - Referring to
FIGS. 9 through 14 ,FIGS. 9 through 14 are schematic views illustrating a method for forming an oxide thin film transistor in accordance with the second embodiment of the present invention. The method will be described in detail accompanying withFIGS. 9 through 14 as follows. - Referring to
FIG. 9 , asubstrate 20 is provided. Thesubstrate 20 has anupper surface 201 for supporting other layers sequentially formed thereon. According to different applications, thesubstrate 20 can comprise different materials, for example, silicon, acrylic resin, or glass. For TFT LCD or EPD applications, thesubstrate 20 can be a transparent substrate such as a glass substrate. - Referring to
FIG. 10 , asource electrode 21 and adrain electrode 22 are formed on thesubstrate 20. Thesource electrode 21 and thedrain electrode 22 can comprise doped silicon, copper or aluminum, or metal compounds such as titanium nitride, tungsten titanium. - Referring to
FIG. 11 , then anoxide semiconductor layer 23 is formed on thesubstrate 20 to connect thesource electrode 21 and thedrain electrode 22. Theoxide semiconductor layer 23 is the channel layer of the transistor to be formed, and can comprise zinc oxide, zinc tin oxide, chromium tin oxide, gallium tin oxide, titanium tin oxide, indium gallium zinc oxide, copper aluminum oxide, strontium copper oxide, and lanthanum copper oxysulfide. In the present embodiment, theoxide semiconductor layer 23 can comprise indium gallium zinc oxide, and a flow rate of argon gas used in the process for forming the indium gallium zinc oxide is 50 SCCM, an electric power is 3.5 KW, a volume ratio of oxygen in the reacting gas for forming the indium gallium zinc oxide is 9%. - Referring to
FIG. 12 , a first depositing process is performed to form agate dielectric layer 24 to cover thesubstrate 20, thesource electrode 21, thedrain electrode 22, and theoxide semiconductor layer 23. Thegate dielectric layer 24 is preferably, but not limited to be, comprised of silicon oxide. Generally, silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NOx) as an oxygen source. The first depositing process includes physical vapor deposition and chemical vapor deposition. - In the present embodiment, the first depositing process is plasma enhanced chemical vapor deposition (PECVD), and a reacting gas used in the PECVD process includes silane and nitrogen oxygen. A flow rate of nitrous oxide is in the range from 10 to 200 standard cubic centimeters per minute (SCCM) such that the obtained
gate dielectric layer 12 has better performance. In other embodiment, a flow rate of nitrous oxide is in the range from 0.5 to 5 SCCM, an electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW. The thickness of the obtainedgate dielectric layer 12 is in the range from 300 angstroms (Å) to 5000 Å. - Referring to
FIG. 13 , agate electrode 25 corresponding to theoxide semiconductor layer 23 is formed ongate dielectric layer 24. Thegate electrode 25 can be formed by depositing a layer of electrically conductive material ongate dielectric layer 24 and then pattering the layer of electrically conductive material. For example, the electrically conductive material can be doped silicon, aluminum, and copper; or metal compound such as titanium nitride or tungsten titanium. - Referring to
FIG. 14 , a second depositing process is performed to form aprotective layer 26 to cover thegate electrode 25 and thegate dielectric layer 24. Theprotective layer 26 can comprise, but is not limited to, silicon oxide. Generally, silicon oxide can be deposited by employing an organic silicon compound, for example, tetraethoxysilane (TEOS), or silane as a silicon source and an oxidant, for example oxygen, ozone, oxynitride (NOx) as an oxygen source, and the depositing process for silicon oxide can be physical vapor deposition or chemical vapor deposition. - In the present embodiment, the second depositing process is PECVD process, the reacting gas includes silane and nitrous oxygen and the flow rate of nitrous oxygen is in the
range 10 SCCM to 200 SCCM. The flow rate of silane is in the range from 0.5 SCCM to 5 SCCM. The electric power applied in the PECVD process is in the range from 0.5 KW to 10 KW. The thickness of the obtainedgate dielectric layer 24 is in the range from 300 Å to 5000 Å. According to above method, a top gate oxide thin film transistor is obtained. - Because the structure of transistor can affect the electron mobility of semiconductors, the top gate transistor is better than bottom gate transistor in this consideration. However, in general TFT LCD applications, considering the requirements of transmitting type display devices and aperture ratio, the bottom gate transistor is also acceptable. Both top gate transistors and bottom gate transistors can be applied in reflective display devices, in particular electro-phoretic display devices.
- Above described embodiments disclose a method for forming an oxide thin film transistor. According to measuring results, the oxide thin film transistor manufactured using above method has advantages of low current leakage, high electron mobility, and other integrated circuit member can be directly formed on the thin film transistor array substrate of a display device.
- The above description is given by way of example, and not limitation. Given the above disclosure, one skilled in the art could devise variations that are within the scope and spirit of the invention disclosed herein, including configurations ways of the recessed portions and materials and/or designs of the attaching structures. Further, the various features of the embodiments disclosed herein can be used alone, or in varying combinations with each other and are not intended to be limited to the specific combination described herein. Thus, the scope of the claims is not to be limited by the illustrated embodiments.
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TWI476935B (en) * | 2012-10-03 | 2015-03-11 | Nat Applied Res Laboratories | Method for fabricating thin film transistor |
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Cited By (5)
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US8829515B2 (en) | 2012-05-16 | 2014-09-09 | Samsung Electronics Co., Ltd. | Transistor having sulfur-doped zinc oxynitride channel layer and method of manufacturing the same |
US9312391B2 (en) | 2013-03-27 | 2016-04-12 | Samsung Electronics Co., Ltd. | Solution composition for forming oxide semiconductor, and oxide semiconductor and electronic device including the same |
US20140354609A1 (en) * | 2013-05-30 | 2014-12-04 | Sharp Kabushiki Kaisha | Liquid crystal display device and method of driving liquid crystal display device |
EP3241234A1 (en) * | 2014-12-30 | 2017-11-08 | Snaptrack, Inc. | Atomic layer deposition of p-type oxide semiconductor thin films |
EP3241234B1 (en) * | 2014-12-30 | 2022-03-23 | Snaptrack, Inc. | Atomic layer deposition of p-type oxide semiconductor thin films |
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